Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1106766
R3HDM2
0.882 0.120 12 57415673 intron variant C/T snv 0.19 7
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs9275596 0.827 0.280 6 32713854 upstream gene variant C/T snv 0.66 7
rs1524107
IL6-AS1 ; IL6
0.827 0.320 7 22728600 non coding transcript exon variant C/T snv 9.4E-02 6
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs267606743
COL4A1
1.000 0.160 13 110192222 missense variant C/T snv 5
rs2281999
UNC13B
0.925 0.160 9 35381507 intron variant C/T snv 0.35 0.38 3
rs4309
ACE
0.925 0.120 17 63482562 synonymous variant C/T snv 0.46 0.36 3
rs741301
ELMO1
0.925 0.160 7 36878390 intron variant C/T snv 0.59 3
rs146956976
GSN
1.000 0.080 9 121302985 missense variant C/T snv 3.1E-04 4.0E-04 2
rs3729548
SLC2A1
1.000 0.080 1 42934681 intron variant C/T snv 0.32 2
rs653747
LINC00923
15 97659878 intron variant C/T snv 0.48 2
rs739401
CARS1
11 3015094 intron variant C/T snv 0.45 2
rs7704116
PPP2CA
1.000 0.080 5 134216763 intron variant C/T snv 9.9E-02 2
rs17881180
LOC102724449 ; SOD1
21 31659974 non coding transcript exon variant C/T snv 3.8E-02 1
rs9932581
MVD ; CYBA
16 88651945 3 prime UTR variant C/T snv 0.39 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1799864
CCR2
0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs237025
SUMO4 ; TAB2
0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 18
rs121908117
ATRIP ; TREX1 ; ATRIP-TREX1
0.708 0.440 3 48466707 missense variant G/A snv 17
rs1143679
ITGAM
0.732 0.520 16 31265490 missense variant G/A snv 9.7E-02 0.11 14